首页> 外文期刊>Physiology & behavior >Neuropeptide regulation of fear and anxiety: Implications of cholecystokinin, endogenous opioids, and neuropeptide Y
【24h】

Neuropeptide regulation of fear and anxiety: Implications of cholecystokinin, endogenous opioids, and neuropeptide Y

机译:恐惧和焦虑的神经肽调节:胆囊收缩素,内源性阿片类药物和神经肽Y的含义

获取原文
获取原文并翻译 | 示例
           

摘要

The neural circuitry of fear likely underlies anxiety and fear-related disorders such as specific and social phobia, panic disorder, and posttraumatic stress disorder. The primary pharmacological treatments currently utilized for these disorders include benzodiazepines, which act on the GABAergic receptor system, and antidepressants, which modulate the monamine systems. However, recent work on the regulation of fear neural circuitry suggests that specific neuropeptide modulation of this system is of critical importance. Recent reviews have examined the roles of the hypothalamic-pituitary-adrenal axis neuropeptides as well as the roles of neurotrophic factors in regulating fear. The present review, instead, will focus on three neuropeptide systems which have received less attention in recent years but which are clearly involved in regulating fear and its extinction. The endogenous opioid system, particularly activating the μ opioid receptors, has been demonstrated to regulate fear expression and extinction, possibly through functioning as an error signal within the ventrolateral periaqueductal gray to mark unreinforced conditioned stimuli. The cholecystokinin (CCK) system initially led to much excitement through its potential role in panic disorder. More recent work in the CCK neuropeptide pathway suggests that it may act in concordance with the endogenous cannabinoid system in the modulation of fear inhibition and extinction. Finally, older as well as very recent data suggests that neuropeptide Y (NPY) may play a very interesting role in counteracting stress effects, enhancing extinction, and enhancing resilience in fear and stress preclinical models. Future work in understanding the mechanisms of neuropeptide functioning, particularly within well-known behavioral circuits, are likely to provide fascinating new clues into the understanding of fear behavior as well as suggesting novel therapeutics for treating disorders of anxiety and fear dysregulation.
机译:恐惧的神经回路可能是焦虑和与恐惧相关的疾病的基础,例如特定和社交恐惧症,恐慌症和创伤后应激障碍。目前用于这些疾病的主要药物治疗包括作用于GABA能受体系统的苯二氮卓类药物和调节单胺系统的抗抑郁药。但是,有关恐惧神经回路调节的最新研究表明,该系统的特定神经肽调节至关重要。最近的评论检查了下丘脑-垂体-肾上腺轴神经肽的作用以及神经营养因子在调节恐惧中的作用。相反,本综述将集中于近年来很少受到关注的三个神经肽系统,但它们显然参与了对恐惧及其消退的调控。已经证明内源性阿片样物质系统,特别是激活μ阿片样物质受体,可能通过在腹侧导水管周围灰色中充当错误信号来标记未增强的条件刺激,从而调节恐惧的表达和消退。胆囊收缩素(CCK)系统最初因其在惊恐症中的潜在作用而引起了极大的兴奋。 CCK神经肽途径的最新研究表明,它可能与内源性大麻素系统协调一致,共同作用于恐惧抑制和绝种的调控。最后,较早的数据和最近的数据表明,神经肽Y(NPY)可能在抵抗压力影响,增强灭绝和增强恐惧和压力临床前模型中发挥重要作用。理解神经肽功能机制的未来工作,尤其是在众所周知的行为回路中,可能会为理解恐惧行为提供令人着迷的新线索,并为治疗焦虑症和恐惧失调症提供新的疗法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号